# FDA Inspection 840700 - Tensys Medical Inc - July 17, 2013

Source: https://www.keypedia.com/records/fda_inspections/tensys-medical-inc/8f654b56-6b71-4a72-bd58-8e10b0b2233a
Source feed: FDA_Inspections

> FDA Inspection 840700 for Tensys Medical Inc on July 17, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 840700
- Company Name: Tensys Medical Inc
- Inspection Date: 2013-07-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 840700 - 2013-07-17](https://www.keypedia.com/records/fda_inspections/tensys-medical-inc/04135fa6-c4c0-4e93-9937-7bdd28d36a3c)
- [FDA Inspection 724825 - 2011-05-13](https://www.keypedia.com/records/fda_inspections/tensys-medical-inc/d0949181-6d73-4e82-9e9e-c29c80bfb1f2)
- [FDA Inspection 724825 - 2011-05-13](https://www.keypedia.com/records/fda_inspections/tensys-medical-inc/bfa91e65-d2e9-4f16-b5ed-f387611bfe3c)

Company: https://www.keypedia.com/companies/tensys-medical-inc/75564f07-2d06-4c2c-9650-b8febe8b3cbc

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7